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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2167317Generated: November 3, 2026

1-Bromo-2-nitrobenzene → HCID 87210606, compound

https://huagongshe.com/reaction/2167317

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-2-nitrobenzeneHCID 11341—
ReactantPotassium CarbonateHCID 11430—
Reactant1,4-DioxaneHCID 31275—
Reactant[9,10-Di(naphthalen-1-yl)anthracen-2-yl]boronic acidHCID 23160234—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 87210606HCID 87210606—

Reaction Steps

10 g (21.1 mmol) of 9,10-dinaphthylanthracene-2-boronic acid, 10.64 g (52.7 mmol) of bromonitrobenzene, 1.21 g (0.05 mmol) of Pd(PPh3)4, and 11.65 g (84.3 mmol) of K2CO3 were diluted with 100 ml of dioxane, 100 ml of THF, and 30 ml of H2O, and then, the mixture was refluxed while heating. After 12 hours, a solvent was removed and the resultant mixture was extracted using MC and washed with a saturated NaCl solution. Then, an organic layer was dried and condensed over MgSO4, and the obtained product was purified by column chromatography (MC/Hex=1/5), thereby producing 2-(2-nitrophenyl)-9,10-di(2-naphthyl)anthracene that was yellow solid (8.4 g, 73%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045419B2
Source datasetuspto-grants-2015_06
ORD IDord-8b87d5156a3a4774a23e44d227760b5e
Source noteuspto-grants-2015_06